Canonical Allele Identifier: PA2825971408
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2261914
ClinVar RCV Id: RCV002773420
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Trp393Gly
CA382894358
NM_001164277.2:c.1177T>G